Anesthesiology
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- Diagnostic DevicesCFR Sub-Part
- General Hospital and Personal Use Monitoring DevicesCFR Sub-Part
- General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- MiscellaneousMiscellaneous
- Neurological Surgical DevicesCFR Sub-Part
- Physical Medicine Therapeutic DevicesCFR Sub-Part
- Prosthetic DevicesCFR Sub-Part
- Surgical DevicesCFR Sub-Part
- Therapeutic DevicesCFR Sub-Part
- NGUBalloon, Liver Tamponade2Product Code
- EYRTourniquet, Gastro-Urology1Product Code
- EXMTruss, Umbilical1Product Code
- EYNTray, Irrigation, Sterile2Product Code
- FBQTrocar, Gastro-Urology2Product Code
- FZGApparatus, Air Handling, Bench2Product Code
- FZHApparatus, Air Handling, Room2Product Code
- FZIApparatus, Air Handling, Enclosure2Product Code
- GAXTourniquet, Nonpneumatic1Product Code
- KCWEpilator, High Frequency, Needle-Type1Product Code
- KCXEpilator, High Frequency, Tweezer-Type1Product Code
- KCYTourniquet, Pneumatic1Product Code
- K202919ATS 5000 Automatic Tourniquet Instrument1Cleared 510(K)
- K162365T-Cuff1Cleared 510(K)
- K123553ZIMMER A.T.S. 4000TS AUTOMATIC TOURNIQUET SYSTEM1Cleared 510(K)
- K112874EZ VEIN INFLATABLE TOURNIQUET1Cleared 510(K)
- K071140MRI COMPATIBLE THIGH TOURNIQUET, MODEL C0700021Cleared 510(K)
- K050411ZIMMER A.T.S. 3000 AUTOMATIC TOURNIQUET SYSTEM1Cleared 510(K)
- K012632TOURNIQUET CUFF; PNEUMATIC TOURNIQUET1Cleared 510(K)
- K955552EXPRESSAIRE TORUNIQUET SYSTEM1Cleared 510(K)
- K954201BUONAFEDE PNEUMATIC SLEEVE1Cleared 510(K)
- K954103TOURNI-COMP1Cleared 510(K)
- Show All 34 Submissions
- KPJChamber, Oxygen, Topical, Extremity2Product Code
- OJSTourniquet Kit1Product Code
- OLIFat Reducing Low Level Laser2Product Code
- PKTLaser For Disruption Of Adipocyte Cells For Aesthetic Use2Product Code
- QGXGeneral Use Pneumatic Tourniquet1Product Code
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
EZ VEIN INFLATABLE TOURNIQUET
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K112874
- 510(k) Type
- Traditional
- Applicant
- DOMINION MEDICAL DEVICES, LLC
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 10/17/2011
- Days to Decision
- 17 days
- Submission Type
- Summary